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Triglyceride levels

near RNU6-376P · rs749804194

What the study found

Who was studied 1,320,016 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.828 lower (95% confidence interval 0.67-0.99); p = 2 × 10−16.

How common The C allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 11, band 11q23.3 — between genes, 1.2 kb from RNU6-376P.

What each result means

C/C Two copies of the version the research linked to Triglyceride levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Triglyceride levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Triglyceride levels. This is the starting point the study compared everyone against.
Source

Questions about rs749804194

What is rs749804194?

rs749804194 is a single position in the genome, in or near the near RNU6-376P gene. Published research associates it with triglyceride levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs749804194 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs749804194 come from?

GWAS Catalog, Nature 2021, PMID:34887591. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Triglyceride levels (rs749804194). MyGeneLog™. https://www.mygenelog.com/variants/rs749804194

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